Hokuriku University, Kanazawa, Japan.
Nicotine Tob Res. 2013 Feb;15(2):572-82. doi: 10.1093/ntr/nts149. Epub 2012 Sep 4.
The aim of this review was to report an update of a previous meta-analysis (by another group) of a possible relationship between serotonin transporter (5-HTTLPR) genotype and smoking behavior, and extend previous work by factoring in some demographic parameters (age, gender, and ethnicity) in a multiple regression model to examine the relationship between these demographic factors and the effect of 5-HTTLPR polymorphism on smoking behavior.
Effect sizes were calculated for each study selected for meta-analysis and were pooled using the random-effects model, which assumes within-study sampling and between-study variance and provides wider confidence intervals. Effect sizes calculated in each study were used to evaluate the correlations with participant data for age, gender, and ethnicity (moderating variable) by multiple regression analysis.
Meta-analysis indicated a relationship between smoking rate and the 5-HTTLPR genotype, but not smoking initiation and persistence, which was consistent with that of the previous review. Publication bias was not indicated for smoking initiation or persistence. Multiple regression analysis revealed that mean participant age significantly affected effect sizes for smoking initiation and persistence of each study. The proportion of Caucasians may have been partially influenced by the difference in effect sizes for smoking persistence among the studies.
A significant relationship stratified by ancestry was observed between the 5-HTTLPR genotype and smoking rate, but not between the 5-HTTLPR genotype and smoking initiation and persistence. Regression analysis detected effects of age and/or ethnicity as moderating factors on smoking initiation and persistence.
本综述旨在报告先前一项关于血清素转运体(5-HTTLPR)基因型与吸烟行为之间可能存在关联的荟萃分析(由另一组进行)的更新,并通过在多元回归模型中加入一些人口统计学参数(年龄、性别和种族)来扩展先前的工作,以检验这些人口统计学因素与 5-HTTLPR 多态性对吸烟行为的影响之间的关系。
为每个入选的荟萃分析研究计算效应大小,并使用随机效应模型进行汇总,该模型假设研究内抽样和研究间变异性,并提供更广泛的置信区间。在每个研究中计算的效应大小用于通过多元回归分析评估与参与者年龄、性别和种族(调节变量)的数据的相关性。
荟萃分析表明吸烟率与 5-HTTLPR 基因型之间存在关系,但与吸烟起始和持续时间无关,这与先前的综述一致。没有发现吸烟起始或持续时间的发表偏倚。多元回归分析显示,平均参与者年龄显著影响每个研究的吸烟起始和持续时间的效应大小。白种人比例可能部分受到研究中吸烟持续时间的效应大小差异的影响。
在血统分层的情况下,观察到 5-HTTLPR 基因型与吸烟率之间存在显著关系,但与 5-HTTLPR 基因型与吸烟起始和持续时间之间没有关系。回归分析检测到年龄和/或种族作为吸烟起始和持续时间的调节因素的影响。